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chr8_143927053_T_C

chr8:143927053 · GRCh38TCrs200895043gnomAD AF 5.04e-3receptor_confirmed

For a non-coding regulatory variant the nearest gene by distance is frequently not the regulated gene.

Receptor variant-effect scores

PXR
0.905GoF
FXR
0.895GoF
AhR
0.876GoF
-1 (LoF)0+1 (GoF)

Strongest effect: PXR GoF at normalized 0.905. Impact is high, in the upper range toward the 99th percentile.

ft_head_delta_norm = center bin sum of ALT minus REF on the receptor CHIP_TF head, normalized to the peak population 99th percentile and clipped to [−1, 1]. AhR is reported as exploratory, single replicate.

Cross-annotations

ClinVar
Benign/Likely benign · not specified · record
phyloP conservation
3.09 · conserved
gnomAD
AF 5.04e-3 · browser
dbSNP
rs200895043
Region tier
receptor_confirmed

Mirrored from ClinVar, GTEx, GWAS Catalog, JASPAR/FIMO, gnomAD and phyloP. See Databases.

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
TA0.5840.5530.588not observed
TC0.9050.8950.8765.0e-3
TG0.8470.8430.797not observed

Every possible base substitution at chr8:143927053, each scored independently. The gnomAD column shows which substitution is actually seen in the population versus in silico only. Region confidence is the same for every substitution at this position, so it is shown once in the section below.

Region confidence

In receptor peaks: FXR

Multi receptor overlap: FXR

Binding motif

Logo for the strongest scoring receptor, PXR. The highlighted column marks the approximate affected base within the response element. External browser: UCSC Genome Browser.